FDA inspection
COVIDIEN FORMERLY MALLINCKRODT DAR S.R.L.: FDA inspection ending Jul 12, 2001
FDA inspection 83219 · No Action Indicated (NAI) · Mirandola
Key facts
| Inspection ID | 83219 |
|---|---|
| Firm | COVIDIEN FORMERLY MALLINCKRODT DAR S.R.L. |
| FEI number | 3002808696 |
| Address | 2/4/6/8 |
| City | Mirandola |
| Fiscal year | 2001 |
| Inspection end date | Jul 12, 2001 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data